8 дней назад
Associate Director, Clinical Science & External Research (MedTech)
137 000 - 235 750$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Associate Director, Clinical Science & External Research (MedTech): Leading end-to-end external research programs, clinical trials, post-market studies, and publication planning for electrophysiology products with an accent on clinical evidence generation, scientific communications, and cross-functional execution. Focus on managing investigator-led research, developing publication strategies, ensuring GCP and ICMJE compliance, and mentoring clinical science staff.
Location: Irvine, California, United States; hybrid work arrangement; up to 15% travel may be required.
Salary: $137,000–$235,750 per year
Company
Johnson & Johnson MedTech develops innovative, less invasive and personalized healthcare solutions, including cardiovascular and electrophysiology products.
What you will do
- Lead end-to-end management of external research projects, clinical trials and post-market studies.
- Develop and execute clinical evidence generation and publication strategies with Clinical Research, Biostatistics, investigators and physician authors.
- Draft and edit scientific publications and presentations while enforcing company policies, SOPs, GCP and ICMJE standards.
- Coordinate clinical trial procedures, sponsor activities, investigator relationships, study timelines, budgets and management reporting.
- Partner with Medical Affairs, Data Science, Health Economics and Market Access, Marketing, Education and Communications teams.
- Supervise and mentor team members and junior Clinical Science & External Research staff.
Requirements
- Bachelor’s or Master’s degree in Life Science, Physical Science, Nursing, Biological Science or a related field with 10–12 years of relevant experience; or PhD, MD or PharmD with 8–10 years of industry or academic research experience.
- At least 5 years of clinical research, clinical publication planning and medical writing experience.
- Experience leading teams in clinical research or evidence generation strategy.
- Advanced project management, analytical, prioritization and communication skills.
- Working knowledge of biostatistical methods, Good Clinical Practice and ICMJE standards.
- Must work from Irvine, California, United States.
Nice to have
- Medical device experience, particularly cardiovascular or electrophysiology experience.
- Pre-market or post-market study design and execution experience.
- Experience with medical writing and publication planning.
Culture & Benefits
- Inclusive work environment focused on diversity, dignity and equal opportunity.
- Vacation, sick time, holiday pay, personal and family time, parental leave and caregiver leave.
- Volunteer leave, bereavement leave and military spouse time off are available according to company policies.
- Opportunity to collaborate with international teams and external physician partners.
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